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WELL LEAD REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073383
510(k) Type
Traditional
Applicant
WELL LEAD MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2008
Days to Decision
220 days
Submission Type
Summary

WELL LEAD REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073383
510(k) Type
Traditional
Applicant
WELL LEAD MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2008
Days to Decision
220 days
Submission Type
Summary